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Bioinformatics for NGS - Webinars/ Tutorials/ Videos

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Bioinformatics for NGS - Webinars/ Tutorials/ Videos


Bioinformatics

Avadis NGS webinars on Youtube

Avadis provides a list of webinars that explain the different applications of the Avadis application software and workflow.

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Avadis NGS analysis workflow

This webinar gives a commercial introduction of the Avadis NGS analysis workflow with focus on SNP call and the corresponding analysis tool.

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CentoMD®3.0 - The largest mutation database of rare diseases

CentoMD® features a comprehensive and unique repository of genetic variants including a significant number of unpublished relevant variants from a worldwide cohort of patients.

In this webinar, Dr. Oprea will demonstrate CentoMD® features and how using this unique database can help you to increase your diagnostic rates. During the webinar, you will learn how CentoMD® 3.0 will become your simple five-step solution, where you easily can search, filter, select, explore and download genes, transcripts and variants and ending with a comprehensive genetic summary including all associated data tailored to your needs.

Source: Centogene

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DNASTAR - Optimizing Illumina and Ion Torrent Data for the Most Accurate NGS Assemblies

This webinar gives a commercial introduction to the seqman ngen from DNASTAR. software for SNP calls.

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DNASTAR webinars on Youtube

DNASTAR provides a list of webinars that describe the usage of different analysis tools and discusses this with different application examples.

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Next-Gen Sequencing Data Management, Assembly, and Analysis

A 46 min commercial product introduction from DNASTAR (2015). It is about the DNASTAR cloud and different options like enabling of assemblies, computer working power rental and data storage. The system is based on amazone workspace computer.

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NGS Informatics and Interpretation — Hardware Considerations data analysis hardware and software

This is an commercial introduction to the knoSYS k100/ 25 systems. The knoSYS system offers a solution for data analysis and storage. This tutorial gives an overview about the requirements needed to build up the infrastructure for sequencing data generation and analysis. The webinar might be especially interesting for labs who want to built up their own sequencing and data analysis workflow.

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Statistics for Genomics: Intro to Next Generation Sequencing

This is an introduction to the basics of NGS more useful for beginners that plan to use the technology. The 34 minute video is from 2012.

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The Importance of Bioinformatics in NGS

Unprecedented advances have been made in the speed and throughput of next generation sequencing (NGS) platforms over the last decade. This progress has imposed increasingly high demands on the bioinformatics tools necessary for analysis of the data generated, which has grown exponentially. Although hundreds of thousands of samples have been sequenced, our ability to find, associate, and implicate genetic variants and candidate disease genes far outstrips our ability to understand them. Many researchers are comfortable with NGS technology, but encounter difficulties with the bioinformatics portion of their workflow, rendering NGS a less attractive option as their primary sequencing platform. However, once clear bioinformatics procedures are established and optimized this bottleneck can be removed, resulting in smooth and routine data interpretation processes and expedited research discoveries. During this webinar, our expert speakers will discuss their bioinformatics strategies and applications in range of fields of clinical research.

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The Next Generation of Pathway Analysis for Integrated Omics Data MetaCore™

MetaCore™ addresses the issue of contextual biology across a wide range of disciplines by providing an integrated software suite for functional analysis of next-gen sequencing, variant, CNV, microarray, metabolic, SAGE, proteomics, siRNA, microRNA, and screening data. A registration is needed.

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Variant Analysis Tips and Tricks

This 66 min webinar (2014) introduces the ingenuity variant analysis software tool from Qiagen. During the webinar you will get analysis setup tips, learn to identify and remove artefacts. It is discussed how to use variant filtering and algorithms for assessing of variants. It is also explained how you can save settings as template for further analysis.

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